Does (CUG)n repeat in DMPK mRNA ‘paint’ chromosome 19 to suppress distant genes to create the diverse phenotype of myotonic dystrophy?:
- 17 February 2001
- journal article
- Published by Springer Nature in neurogenetics
- Vol. 3 (2) , 59-67
- https://doi.org/10.1007/s100480000103
Abstract
No abstract availableKeywords
This publication has 52 references indexed in Scilit:
- Mice deficient in Six5 develop cataracts: implications for myotonic dystrophyNature Genetics, 2000
- Heterozygous loss of Six5 in mice is sufficient to cause ocular cataractsNature Genetics, 2000
- DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy modelJournal of Clinical Investigation, 1999
- Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP geneNature Genetics, 1997
- Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHPNature Genetics, 1997
- Anticipating anticipationNature Genetics, 1997
- Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathyNature Genetics, 1996
- Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in miceNature Genetics, 1996
- Myotonic dystrophy: evidence for a possible dominant-negative RNA mutationHuman Molecular Genetics, 1995
- Genomic organization and transcriptional units at the myotonic dystrophy locusGenomics, 1993